Medical Advisor

Responsibilities

• Oversee the direction, planning, and execution of clinical trials and research activities
• Contribute to the implementation of clinical protocols and facilitate the completion of final reports
• Recruit clinical investigators and negotiate study design and costs
• Direct human clinical trials, specifically phases III and IV, for products under development
• Monitor adherence to protocols and determine study completion
• Participate in adverse event reporting and safety monitoring responsibilities
• Coordinate and provide reporting information for submissions to regulatory agencies
• Act as a consultant or liaison with other corporations under licensing agreements

Requirements

• Minimum of 7 years of relevant professional experience
• Associates Degree or equivalent higher education
• Extensive knowledge of clinical protocols
• Proven experience in clinical trial management

About the Company

Abbott is a global healthcare leader that has been helping people reach their potential for more than 135 years. With a network serving customers in more than 160 countries, Abbott creates innovative solutions across diagnostics, medical devices, science-based nutrition, and branded generic pharmaceuticals to help people live their best lives through better health.